Veeva Systems

NEW WEBINAR: Revolutionize Your GxP Training Translations Tired of the hassle of traditional GxP training translations? Discover how we leveraged AI to streamline our process, saving time, money, and resources! REGISTER HERE ➡️ https://lnkd.in/evyX_-6i Join our webinar to discover: ⭐️ The power of AI for GxP training translations. ⭐️ The benefits of global accessibility for your training programs. ⭐️ How to streamline your translation process, and save time & resources with LearnGxP. Don't miss out! Register now to learn how to revolutionize your GxP training translations. #GxP #pharma #biotech #translation #AI #webinar #elearning #globalization

Best part of Veeva placing in Newsweek's Top 100 Most Reliable Companies list is that it comes from earning the trust of so many companies we work with who added us to the list. Honored that our focus on supporting customers to advance the #lifesciences industry is recognized. Check out the full list here: https://bit.ly/4eUJpIn #lifeatveeva #careers

We're excited to have Sean Casey keynote our Clinical Data Forum on November 14. Sean will share strategies for adoption and how they connected their EDC, CTMS, and Safety systems to improve #data quality. Our lineup of speakers also includes innovative data leaders from Atorus Research, BeiGene, and Faro Health. Ready to see what's coming next in #clinicaldatamanagement? View the agenda and register today to secure your free spot, link will be shared in the comments. We have limited seats available!

I am counting down the days until our next Clinical Data Innovation Forum in the San Francisco Bay Area on November 14. We have a great lineup of speakers including Sean Casey from Inhibrx Biosciences, Inc. who will share how they brought their EDC, CTMS, and Safety systems in-house and managed change and adoption of new systems at scale. Meg Richie will also be there to discuss the future of #datamanagement and how we get there. These events are designed to maximize connections, and we are excited to bring the community together to discuss what’s next for #clinicaldatamanagent. Register here for this complimentary event: https://lnkd.in/ePEpftWX. Seats are limited!

The journey to omnichannel begins with a strong content foundation. 📑 Learn how BioMarin Pharmaceutical Inc. analyzed its content quality and flow to achieve a seamless customer experience. https://bit.ly/4eFXU2l #pharmaceuticals #contentstrategy

We're one week away from World Drug Safety Congress Americas in Boston! See how biopharmas, from emerging to top 20, are driving operational efficiencies and empowering safety teams with real-time data at booth #431. It's not too late to book a meeting with a safety expert at WDSC: https://lnkd.in/e_3FduNS #wdsc #veeva #vaultsafety

With more treatments being delivered in-office, legacy data is creating blind spots for biopharmas as it only covers prescription activity. Hear life sciences GTM leaders from Acuitas360, Amazon Web Services (AWS), and Veeva discuss how they use modern patient data to generate a complete view of the market to better inform: - Segmentation and Targeting - Forecasting - Customer journey mapping Join us October 24th: https://lnkd.in/gwvYTMAT #biopharma #lifesciences #VeevaCompass

🚀 Driving Seamless Sponsor-Site Collaboration in Clinical Trials 🚀 In a recent interview with Kenny Kong, Vice President of Strategy for Veeva Systems Site Connect, we discussed the challenges in sponsor-site collaboration and how Veeva is breaking down barriers with innovative solutions. 💡 Key insights: • Fragmented Technology: Disconnected systems between sponsors and sites lead to inefficiencies. Veeva addresses this by standardizing processes and creating a unified platform. • Interoperability: A common data framework is essential for seamless data exchange, reducing errors and speeding up trials. • Site Experience: By simplifying administrative tasks, Veeva enables sites to focus more on patient care, expediting approvals and improving performance. #clinicaltrials #innovation #healthcare #Veeva #SiteConnect #collaboration #clinicalresearch Deivis Mercado

In our recent interview with Carolyn Jin, Director of Clinical Systems and Document Management at Kura Oncology, Inc., she shared valuable insights into how eTMF is transforming clinical trials by improving CRO partnerships, enhancing oversight, and ensuring regulatory compliance. Key Highlights: • Collaborative eTMF systems foster better alignment with CROs, improving transparency and efficiency. • A risk-based oversight approach focuses on high-risk documents, ensuring compliance without added workload. • Scalability of eTMF systems allows small teams to manage multiple trials efficiently. • eTMF provides a complete, searchable digital trial narrative, making regulatory reviews seamless. • AI has the potential to further enhance scalability and efficiency in the future. #eTMF #ClinicalTrials #CRO #Compliance #RiskBasedOversight #DigitalTransformation #AI #ClinicalOperations Veeva Systems Deivis Mercado